Three dimensional adjuncts

ABSTRACT

Stapling assemblies for use with a surgical stapler and methods for manufacturing the same are provided. Three dimensional adjuncts for use with a surgical stapling assembly and methods for manufacturing the same are also provided.

FIELD

Three dimensional adjuncts and methods for manufacturing the same areprovided.

BACKGROUND

Surgical staplers are used in surgical procedures to close openings intissue, blood vessels, ducts, shunts, or other objects or body partsinvolved in the particular procedure. The openings can be naturallyoccurring, such as passageways in blood vessels or an internal organlike the stomach, or they can be formed by the surgeon during a surgicalprocedure, such as by puncturing tissue or blood vessels to form abypass or an anastomosis, or by cutting tissue during a staplingprocedure.

Some surgical staplers require a surgeon to select the appropriatestaples having the appropriate staple height for the tissue beingstapled. For example, a surgeon could select tall staples for use withthick tissue and short staples for use with thin tissue. In someinstances, however, the tissue being stapled does not have a consistentthickness and, thus the staples cannot achieve the desired firedconfiguration at each staple site. As a result, a desirable seal at ornear all of the stapled sites cannot be formed, thereby allowing blood,air, gastrointestinal fluids, and other fluids to seep through theunsealed sites.

Further, staples, as well as other objects and materials that can beimplanted in conjunction with procedures like stapling, generally lacksome characteristics of the tissue in which they are implanted. Forexample, staples and other objects and materials can lack the naturalflexibility of the tissue in which they are implanted, and therefore areunable to withstand the varying intra-tissue pressures at theimplantation site. This can lead to undesirable tissue tearing, andconsequently leakage, at or near the staple site.

Accordingly, there remains a need for improved instruments and methodsthat address current issues with surgical staplers.

SUMMARY

Stapling assemblies for use with a surgical stapler are provided.

In one exemplary embodiment, a stapling assembly is provided and caninclude a body having a first end and a second end, and a longitudinalaxis extending therebetween. The body can have a slot that extends intoand along at least a portion of the longitudinal axis and can beconfigured to receive a cutting element. The stapling assembly can alsoinclude a three-dimensional compressible adjunct formed from a matrixthat includes at least one fused bioabsorbable polymer, and the adjunctcan be configured to be releasably retained on the body. The adjunct caninclude a plurality of struts, and the adjunct can have a longitudinalchannel extending therealong between a first longitudinal portion and asecond longitudinal portion. The first and second longitudinal portionscan be configured to be positioned on opposite sides of the slot withthe channel extending along the slot of the body to facilitate cuttingalong the longitudinal channel as the cutting element moves through theslot.

In some aspects, the channel can have one or more openings extendingtherethrough. In other aspects, at least a portion of the channel can becut as the cutting element distally advances through the slot.

In one aspect, the body can also include a plurality of staples disposedtherein. The plurality of staples can be configured to be deployed intotissue such that the adjunct can be attached to tissue by the pluralityof staples.

In another aspect, the adjunct can be configured to apply a stress of atleast about 3 g/mm² to the tissue stapled thereto for at least 3 dayswhen the adjunct is in a tissue deployed state.

The plurality of struts can have a variety of configurations. Forexample, the plurality of struts can be interconnected at nodes to formtruss-like structures. In one embodiment, the plurality of struts can besubstantially spiral-shaped. In another embodiment, the plurality ofstruts can be in the form of substantially vertical columns.

In another exemplary embodiment, a stapling assembly can be providedthat includes a body having a first end and a second end, and alongitudinal axis extending therebetween. The body can have a slot thatextends into and along at least a portion of the longitudinal axis andcan be configured to receive a cutting element. The stapling assemblycan also include a three-dimensional compressible adjunct formed from amatrix that includes at least one fused bioabsorbable polymer. Theadjunct can have interconnected struts that form a lattice structurehaving first and second longitudinal portions that are connected by atleast one bridging member. The at least one bridging member can beconfigured to facilitate advancement of the cutting element through theadjunct.

In some aspects, when the adjunct is releasably retained on the body,the at least one bridging member can extend across the slot in a lateraldirection relative to the longitudinal axis of the body such that distaladvancement of the cutting element can cut through the at least onebridging member.

In other aspects, the fused one or more bioabsorbable polymers caninclude a first fused bioabsorbable polymer and a second fusedbioabsorbable polymer that is stiffer than the first fused bioabsorbablepolymer. The first and second portions can be formed of the first fusedbioabsorbable polymer and the at least one bridging member can be formedof the second fused bioabsorbable polymer.

In certain aspects, the body can also include a plurality of staplesdisposed therein. The plurality of staples can be configured to bedeployed into tissue such that the adjunct can be attached tissue by theplurality of staples.

In one aspect, the adjunct can be configured to apply a stress of atleast about 3 g/mm² to the tissue stapled thereto for at least 3 dayswhen the adjunct is in a tissue deployed state.

BRIEF DESCRIPTION OF THE DRAWINGS

This invention will be more fully understood from the following detaileddescription taken in conjunction with the accompanying drawings, inwhich:

FIG. 1 is a perspective view of one exemplary embodiment of aconventional surgical stapling and severing instrument;

FIG. 2 is a perspective view of a wedge sled of a staple cartridge ofthe surgical stapling and severing instrument of FIG. 1;

FIG. 3 is a perspective view of a knife and firing bar (“E-beam”) of thesurgical stapling and severing instrument of FIG. 1;

FIG. 4 is a longitudinal cross-sectional view of a surgical cartridgethat can be disposed within the stapling and severing instrument of FIG.1;

FIG. 5 is a top view of a staple in an unfired (pre-deployed)configuration that can be disposed within the staple cartridge of thesurgical cartridge assembly of FIG. 4;

FIG. 6 is a longitudinal cross-sectional view of an exemplary embodimentof a surgical cartridge assembly having an adjunct attached to acartridge deck;

FIG. 7 is a schematic illustrating the adjunct of FIG. 6 in a tissuedeployed condition;

FIG. 8A is a perspective view of one exemplary embodiment of an adjuncthaving a plurality of repeating units of interconnected struts;

FIG. 8B is a magnified view of a repeating unit of the adjunct shown inFIG. 8A taken at 8B;

FIG. 9A is a schematic illustration of the repeating unit of FIG. 8B ina precompressed state;

FIG. 9B is a schematic illustration of the repeating unit of FIG. 8B ina first compressed state;

FIG. 9C is a schematic illustration of the repeating unit shown of FIG.8B in a second compressed state;

FIG. 10 is a graphical illustration of the relationship betweenstiffness and compression of an adjunct;

FIG. 11A is a perspective view of an exemplary embodiment of an adjuncthaving a plurality of interconnected struts and inner connectivityfeatures;

FIG. 11B is a perspective cross-sectional view of the adjunct shown inFIG. 11A taken at 11B;

FIG. 12A is a perspective view of another exemplary embodiment of anadjunct having a plurality of interconnected struts and linking members;

FIG. 12B is a magnified view of a repeating unit of the adjunct shown inFIG. 12A taken at 12B;

FIG. 13A is a perspective view of another exemplary embodiment of anadjunct having a plurality of struts of a first material that areinterconnected at joints or nodes of a second material;

FIG. 13B is a magnified view of a repeating unit of the adjunct shown inFIG. 13A taken at 13B;

FIG. 14 is a perspective view of yet another exemplary embodiment of arepeating unit of interconnected struts with end shapes;

FIG. 15 is a perspective view of an adjunct according to anotherembodiment having a plurality of struts and at least one stoppingelement;

FIG. 16 is a perspective view of an exemplary embodiment of an adjuncthaving a plurality of struts that are substantially spiral-shaped;

FIG. 17 is a perspective view of another exemplary embodiment of anadjunct that includes a plurality of struts in the form of verticalcolumns having different lengths;

FIG. 18A is a schematic illustration of the adjunct shown in FIG. 17 ata precompressed height;

FIG. 18B is a schematic illustration of the adjunct shown in FIG. 17 ata first compressed height;

FIG. 18C is a schematic illustration of the adjunct shown in FIG. 17 ata second compressed height;

FIG. 19 is a side view of an exemplary embodiment of an adjunct thatincludes a plurality of struts in the form of vertical columns andcurved columns;

FIG. 20 is a graphical representation of the mechanical behavior of theadjunct shown in FIG. 19 over a compression range;

FIG. 21A is a perspective view of another exemplary embodiment of anadjunct having a channel configured to receive a cutting element andhaving tabs for attaching the adjunct to a staple cartridge;

FIG. 21B is an exemplary embodiment of a staple cartridge assemblyhaving the adjunct shown in FIG. 21A attached to a cartridge body; and

FIG. 22 is an exemplary embodiment of an adjunct having bridgingmembers.

DETAILED DESCRIPTION

Certain exemplary embodiments will now be described to provide anoverall understanding of the principles of the structure, function,manufacture, and use of the instruments and methods disclosed herein.One or more examples of these embodiments are illustrated in theaccompanying drawings. Those skilled in the art will understand that theinstruments, systems, and methods specifically described herein andillustrated in the accompanying drawings are non-limiting exemplaryembodiments and that the scope of the present invention is definedsolely by the claims. The features illustrated or described inconnection with one exemplary embodiment may be combined with thefeatures of other embodiments. Such modifications and variations areintended to be included within the scope of the present invention.

Further, in the present disclosure, like-named components of theembodiments generally have similar features, and thus within aparticular embodiment each feature of each like-named component is notnecessarily fully elaborated upon. Additionally, to the extent thatlinear or circular dimensions are used in the description of thedisclosed systems, instruments, and methods, such dimensions are notintended to limit the types of shapes that can be used in conjunctionwith such systems, instruments, and methods. A person skilled in the artwill recognize that an equivalent to such linear and circular dimensionscan easily be determined for any geometric shape. Sizes and shapes ofthe systems and instruments, and the components thereof, can depend atleast on the anatomy of the subject in which the systems and instrumentswill be used, the size and shape of components with which the systemsand instruments will be used, and the methods and procedures in whichthe systems and instruments will be used.

It will be appreciated that the terms “proximal” and “distal” are usedherein with reference to a user, such as a clinician, gripping a handleof an instrument. Other spatial terms such as “front” and “rear”similarly correspond respectively to distal and proximal. It will befurther appreciated that for convenience and clarity, spatial terms suchas “vertical” and “horizontal” are used herein with respect to thedrawings. However, surgical instruments are used in many orientationsand positions, and these spatial terms are not intended to be limitingand absolute.

Values or ranges may be expressed herein as “about” and/or from/of“about” one particular value to another particular value. When suchvalues or ranges are expressed, other embodiments disclosed include thespecific value recited and/or from/of the one particular value toanother particular value. Similarly, when values are expressed asapproximations, by the use of antecedent “about,” it will be understoodthat here are a number of values disclosed therein, and that theparticular value forms another embodiment. It will be further understoodthat there are a number of values disclosed therein, and that each valueis also herein disclosed as “about” that particular value in addition tothe value itself. In embodiments, “about” can be used to mean, forexample, within 10% of the recited value, within 5% of the recited valueor within 2% of the recited value.

For purposes of describing and defining the present teachings, it isnoted that unless indicated otherwise, the term “substantially” isutilized herein to represent the inherent degree of uncertainty that maybe attributed to any quantitative comparison, value, measurement, orother representation. The term “substantially” is also utilized hereinto represent the degree by which a quantitative representation may varyfrom a stated reference without resulting in a change in the basicfunction of the subject matter at issue.

Surgical stapling assemblies and methods for manufacturing the same andfor stapling tissue are provided. In general, a stapling assembly isprovided having a body (e.g., a staple cartridge or end effector body)with a plurality of staples disposed therein. The stapling assembly alsoincludes a three-dimensional compressible adjunct formed from a matrixthat includes at least one fused bioabsorbable polymer and configured tobe releasably retained on the body. The adjunct can be releasablyretained to the body such that when a staple is deployed from the bodyand into tissue, at least a portion of the adjunct can attach to thetissue captured by the staple. As discussed herein, the adjunct can beconfigured to compensate for variations in tissue properties, such asvariations in the tissue thickness, and/or promote tissue ingrowth whenthe adjunct is stapled to tissue. For example, the adjunct can beconfigured to apply a stress of at least about 3 g/mm² to tissue for atleast 3 days when in a tissue deployed state (e.g., when the adjunct isstapled to tissue in vivo).

An exemplary stapling assembly can include a variety of features tofacilitate application of a surgical staple, as described herein andillustrated in the drawings. However, a person skilled in the art willappreciate that the stapling assembly can include only some of thesefeatures and/or it can include a variety of other features known in theart. The stapling assemblies described herein are merely intended torepresent certain exemplary embodiments. Moreover, while the adjunctsare described in connection with surgical staple cartridge assemblies,and need not be replaceable, the adjuncts can be used in connection withstaple reloads that are not cartridge based or any type of surgicalinstrument.

FIG. 1 illustrates an exemplary surgical stapling and severinginstrument 100 suitable for use with an implantable adjunct. Theillustrated surgical stapling and severing instrument 100 includes astaple applying assembly 106 or end effector having an anvil 102pivotably coupled to an elongate staple channel 104. The staple applyingassembly 106 can be attached at its proximal end to an elongate shaft108 forming an implement portion 110. When the staple applying assembly106 is closed, or at least substantially closed, the implement portion110 can present a sufficiently small cross-section suitable forinserting the staple applying assembly 106 through a trocar. While theinstrument 100 is configured to staple and sever tissue, surgicalinstruments configured to staple but not sever tissue are alsocontemplated herein.

In various instances, the staple applying assembly 106 can bemanipulated by a handle 112 connected to the elongate shaft 108. Thehandle 112 can include user controls such as a rotation knob 114 thatrotates the elongate shaft 108 and the staple applying assembly 106about a longitudinal axis of the elongate shaft 108, and a closuretrigger 116 which can pivot in front of a pistol grip 118 to close thestaple applying assembly 106. A closure release button 120 can beoutwardly presented on the handle 112 when the closure trigger 116 isclamped such that the closure release button 120 can be depressed tounclamp the closure trigger 116 and open the staple applying assembly106, for example.

A firing trigger 122, which can pivot in front of the closure trigger116, can cause the staple applying assembly 106 to simultaneously severand staple tissue clamped therein. In various instances, multiple firingstrokes can be employed using the firing trigger 122 to reduce theamount of force required to be applied by the surgeon's hand per stroke.In certain embodiments, the handle 112 can include one or more rotatableindicator wheels such as, for example, rotatable indicator wheel 124which can indicate the firing progress. A manual firing release lever126 can allow the firing system to be retracted before full firingtravel has been completed, if desired, and, in addition, the firingrelease lever 126 can allow a surgeon, or other clinician, to retractthe firing system in the event that the firing system binds and/orfails.

Additional details on the surgical stapling and severing instrument 100and other surgical stapling and severing instruments suitable for usewith the present disclosure are described, for example, in U.S. Pat. No.9,332,984 and in U.S. Patent Application Publication No. 2009/0090763,the disclosure of which is incorporated herein by reference in theirentirety. Further, the surgical stapling and severing instrument neednot include a handle, but instead a housing that is configured to coupleto a surgical robot, for example, as described in U.S. application Ser.No. 15/689,198, filed on Aug. 29, 2017 to Frederick E. Shelton et al.,the disclosure of which is incorporated herein by reference in itsentirety.

With reference to FIGS. 2 and 3, a firing assembly such as, for example,firing assembly 228, can be utilized with a surgical stapling andsevering instrument, such as instrument 100 in FIG. 1. The firingassembly 228 can be configured to advance a wedge sled 230 having aplurality of wedges 232 configured to deploy staples from a stapleapplying assembly, like staple applying assembly 106 in FIG. 1, intotissue captured between an anvil, like anvil 102 in FIG. 1, and anelongate staple channel, like channel 104 in FIG. 1. Furthermore, anE-beam 233 at a distal portion of the firing assembly 228 may fire thestaples from the staple applying assembly as well as position the anvilrelative to the elongate staple channel during firing. The illustratedE-beam 233 includes a pair of top pins 234, a pair of middle pins 236which may follow portion 238 of the wedge sled 230, and a bottom pin orfoot 240. The E-beam 233 can also include a sharp cutting edge 242configured to sever the captured tissue as the firing assembly 228 isadvanced distally. In addition, integrally formed and proximallyprojecting top guide 244 and middle guide 246 bracketing each verticalend of the cutting edge 242 may further define a tissue staging area 248assisting in guiding tissue to the sharp cutting edge 242 prior to beingsevered. The middle guide 246 may also serve to engage and fire thestaple applying assembly by abutting a stepped central member 250 of thewedge sled 230 that effects staple formation by the staple applyingassembly.

Referring to FIG. 4, a staple cartridge 400 can be utilized with asurgical stapling and severing instrument, like surgical stapling andsevering instrument 100 in FIG. 1, and can include a cartridge body 402and a plurality of staple cavities 404 within the cartridge body 402. Astaple 406 can be removably positioned in each staple cavity 404. Thestaple 406 in a unfired (pre-deployed, unformed) configuration is shownin more detail in FIG. 5. The staple cartridge 400 can also include alongitudinal channel that can be configured to receive a firing and/orcutting member, e.g., an E-beam, like E-beam 233 in FIG. 3.

Each staple 406 can include a crown (base) 406 _(C) and one or more legs406 _(L) extending from the crown 406 _(C). Prior to the staples 406being deployed, the crowns 406 _(C) of the staples 406 can be supportedby staple drivers 408 positioned within the staple cartridge 400 and,concurrently, the legs 406 _(L) of the staples 406 can be at leastpartially contained within the staple cavities 404. Further, the staplelegs 406 _(L) of the staples 406 can extend beyond the tissue-contactingsurface 410 of the staple cartridge 400 when the staples 406 are intheir unfired positions. In certain instances, as shown in FIG. 5, thetips of the staple legs 406 _(L) can be sharp which can incise andpenetrate tissue.

In some implementations, the staples can include one or more externalcoatings, e.g., a sodium sterate lubricant and/or an antimicrobialagent(s). The antimicrobial agent(s) can be applied to the staples asits own coating or incorporated into another coating, such as alubricant. Non-limiting examples of suitable antimicrobial agentsinclude 5-Chloro-2-(2,4-dichlorophenoxy)phenol, chlorhexidine, silverformulations (like nano-crystalline silver), lauric arginate ethyl ester(LAE), octenidine, polyhexamethylene biguanide (PHMB), taurolidine,lactic acid, citric acid, acetic acid, and their salts.

The staples 406 can be deformed from an unfired position into a firedposition such that the legs 406 _(L) move through the staple cavities404, penetrate tissue positioned between an anvil, like anvil 102 inFIG. 1, and the staple cartridge 400, and contact the anvil. As the legs406 _(L) are deformed against the anvil, the legs 406 _(L) of eachstaple 406 can capture a portion of the tissue within each staple 406and apply a compressive force to the tissue. Further, the legs 406 _(L)of each staple 406 can be deformed downwardly toward the crown 406 _(C)of the staple 406 to form a staple entrapment area in which the tissuecan be captured therein. In various instances, the staple entrapmentarea can be defined between the inner surfaces of the deformed legs andthe inner surface of the crown of the staple. The size of the entrapmentarea for a staple can depend on several factors such as the length ofthe legs, the diameter of the legs, the width of the crown, and/or theextent in which the legs are deformed, for example.

In use, an anvil, like anvil 102 in FIG. 1, can be moved into a closedposition by depressing a closure trigger, like closure trigger 116 inFIG. 1, to advance an E-beam, like E-beam 233 in FIG. 3. The anvil canposition tissue against a tissue-contacting surface 410 of the staplecartridge 400. Once the anvil has been suitably positioned, the staples406 can be deployed.

To deploy staples 406, as discussed above, a staple-firing sled, likesled 230 in FIG. 2, can be moved from a proximal end 400 p toward adistal end 400 d of the staple cartridge 400. As a firing assembly, likefiring assembly 228 in FIG. 3, is advanced, the sled can contact thestaple drivers 408 and lift the staple drivers 408 upwardly within thestaple cavities 404. In at least one example, the sled and the stapledrivers 408 can each include one or more ramps, or inclined surfaces,which can co-operate to move the staple drivers 408 upwardly from theirunfired positions. As the staple drivers 408 are lifted upwardly withintheir respective staple cavities 404, the staples 406 are advancedupwardly such that the staples 406 emerge from their staple cavities 404and penetrate into tissue. In various instances, the sled can moveseveral staples upwardly at the same time as part of a firing sequence.

A person skilled in the art will appreciate that, while adjuncts areshown and described below, the adjuncts disclosed herein can be usedwith other surgical instruments, and need not be coupled to a staplecartridge as described. Further, a person skilled in the art will alsoappreciate that the staple cartridges need not be replaceable.

As discussed above, with some surgical staplers, a surgeon is oftenrequired to select the appropriate staples having the appropriate stapleheight for the tissue that is to be stapled. For example, a surgeoncould select tall staples for use with thick tissue and short staplesfor use with thin tissue. In some instances, however, the tissue beingstapled does not have a consistent thickness and thus, the staplescannot achieve the desired fired configuration for every section of thestapled tissue (e.g., thick and thin tissue sections). The inconsistentthickness of tissue can also lead to undesirable leakage and/or tearingof tissue at the staple site when staples with the same or substantiallyheight are used, particularly when the staple site is exposed tointra-pressures at the staple site and/or along the staple line.

Accordingly, various embodiments of three-dimensionally printed adjunctsare provided that can be configured to compensate for varying thicknessof tissue that is captured within fired (deployed) staples to avoid theneed to take into account staple height when stapling tissue duringsurgery. That is, the adjuncts described herein can allow a set ofstaples with the same or similar heights to be used in stapling tissueof varying thickness (i.e., from thin to thick tissue) while also, incombination with the adjunct, providing adequate tissue compressionwithin and between fired staples. Thus, the adjuncts described hereincan maintain suitable compression against thin or thick tissue stapledthereto to thereby minimize leakage and/or tearing of tissue at thestaple sites.

Alternatively or in addition, the three-dimensionally printed adjunctscan be configured to promote tissue ingrowth. In various instances, itis desirable to promote the ingrowth of tissue into an implantableadjunct, to promote the healing of the treated tissue (e.g. stapledand/or incised tissue), and/or to accelerate the patient's recovery.More specifically, the ingrowth of tissue into an implantable adjunctmay reduce the incidence, extent, and/or duration of inflammation at thesurgical site. Tissue ingrowth into and/or around the implantableadjunct may manage the spread of infections at the surgical site, forexample. The ingrowth of blood vessels, especially white blood cells,for example, into and/or around the implantable adjunct may fightinfections in and/or around the implantable adjunct and the adjacenttissue. Tissue ingrowth may also encourage the acceptance of foreignmatter (e.g., the implantable adjunct and the staples) by the patient'sbody and may reduce the likelihood of the patient's body rejecting theforeign matter. Rejection of foreign matter may cause infection and/orinflammation at the surgical site.

Unlike conventional adjuncts (e.g., adjuncts that are notthree-dimensionally printed, such as woven adjuncts), thesethree-dimensionally printed adjuncts can be formed with microstructures(units) that are consistent and reproducible. That is, unlike with othermethods of manufacture, 3D printing significantly improves control overmicrostructural features such as e.g., placement and connection ofelements. As a result, variability in both the microstructure(s) andattendant properties of the adjunct is decreased, as compared toconventional woven adjuncts. For example, these three-dimensionallyprinted adjuncts can be structured such that they compress apredetermined amount in a substantially uniform matter. The fine controlover the microstructure can also allow the porosity of the adjunct to betailored to enhance tissue ingrowth. Further, these three-dimensionallyprinted adjuncts can be adapted for use with a variety of staples andtissue types.

In general, the adjuncts provided herein are designed and positionedatop a body, like cartridge body 402 in FIG. 4. When the staples arefired (deployed) from the body, the staples penetrate through theadjunct and into tissue. As the legs of the staple are deformed againstthe anvil that is positioned opposite the staple cartridge assembly, thedeformed legs capture a portion of the adjunct and a portion of thetissue within each staple. That is, when the staples are fired intotissue, at least a portion of the adjunct becomes positioned between thetissue and the fired staple. While the adjuncts described herein can beconfigured to be attached to a cartridge body of a staple cartridgeassembly, it is also contemplated herein that the adjuncts can beconfigured to mate with other instrument components, such as a jaw of asurgical stapler. A person of ordinary skill will appreciate that theadjuncts provided herein can be used with replaceable cartridges orstaple reloads that are not cartridge based.

FIG. 6 illustrates an exemplary embodiment of a staple cartridgeassembly 600 that includes a staple cartridge 602 and an adjunct 604.Aside from the differences described in detail below, the staplecartridge 602 can be similar to staple cartridge 400 (FIG. 4) and istherefore not described in detail herein. As shown, the adjunct 604 ispositioned against the staple cartridge 602. The staple cartridge caninclude a cartridge body 606 and a plurality of staples 608 disposedtherein, like staples 406 shown in FIGS. 4 and 5. The staples 608 can beany suitable unformed (pre-deployed) height. For example, the staples608 can have an unformed height between about 2 mm to 4.8 mm. Prior todeployment, the crowns of the staples 608 can be supported by stapledrivers 610.

In the illustrated embodiment, the adjunct 604 can be mated to an outersurface 612, for example a tissue-contacting surface, of the cartridgebody 606. In some embodiments, the outer surface 612 of the cartridgebody 606 can include one or more attachment features. The one or moreattachments features can be configured to engage the adjunct 604 toavoid undesirable movements of the adjunct 604 relative to the cartridgebody 606 and/or premature release of the adjunct 604 from the cartridgebody 606. Exemplary attachment features can be found in U.S. PatentPublication No. 2016/0106427, which is incorporated by reference hereinin its entirety.

The adjunct 604 is compressible to permit the adjunct to compress tovarying heights to thereby compensate for different tissue thicknessthat are captured within a deployed staple. The adjunct 604 has anuncompressed (undeformed), or pre-deployed, height and is configured todeform to one of a plurality of compressed (deformed), or deployed,heights. For example, the adjunct 604 can have an uncompressed heightwhich is greater than the fired height of the staples 608 (e.g., theheight (H) of the fired staple 608 a in FIG. 7). That is, the adjunct604 can have an undeformed state in which a maximum height of theadjunct 604 is greater than a maximum height of a fired staple 608 a(i.e., a staple that is in a formed configuration). In one embodiment,the uncompressed height of the adjunct 604 can be about 10% taller,about 20% taller, about 30% taller, about 40% taller, about 50% taller,about 60% taller, about 70% taller, about 80% taller, about 90% taller,or about 100% taller than the fired height of the staples 608. Incertain embodiments, the uncompressed height of the adjunct 604 can beover 100% taller than the fired height of the staples 608, for example.

The adjunct 604 can be releasably mated to the outer surface 612 of thecartridge body 606. As shown in FIG. 7, when the staples are fired,tissue (T) and a portion of the adjunct 604 are captured by the fired(formed) staples 608 a. The fired staples 608 a each define theentrapment area therein, as discussed above, for accommodating thecaptured adjunct 604 and tissue (T). The entrapment area defined by afired staple 608 a is limited, at least in part, by a height (H) of thefired staple 608 a. For example, the height of a fired staple 608 a canbe about 0.160 inches or less. In some embodiments, the height of afirst stapled 608 a can be about 0.130 inches or less. In oneembodiment, the height of a fired staple 608 a can be from about 0.020inches to 0.130 inches. In another embodiment, the height of a firedstaple 608 a can be from about 0.060 inches to 0.160 inches.

As described above, the adjunct 604 can be compressed within a pluralityof fired staples whether the thickness of the tissue captured within thestaples is the same or different within each fired staple. In at leastone exemplary embodiment, the staples within a staple line, or row, canbe deformed such that the fired height is about 2.75 mm, for example,where the tissue (T) and the adjunct 604 can be compressed within thisheight. In certain instances, the tissue (T) can have a compressedheight of about 1.0 mm and the adjunct 604 can have a compressed heightof about 1.75 mm. In certain instances, the tissue (T) can have acompressed height of about 1.50 mm and the adjunct 604 can have acompressed height of about 1.25 mm. In certain instances, the tissue (T)can have a compressed height of about 1.75 mm and the adjunct 604 canhave a compressed height of about 1.00 mm. In certain instances, thetissue (T) can have a compressed height of about 2.00 mm and the adjunct604 can have a compressed height of about 0.75 mm. In certain instances,the tissue (T) can have a compressed height of about 2.25 mm and theadjunct 604 can have a compressed height of about 0.50 mm. Accordingly,the sum of the compressed heights of the captured tissue (T) and adjunct604 can be equal, or at least substantially equal, to the height (H) ofthe fired staple 608 a.

As discussed in more detail below, the structure of the adjunct can beconfigured such that when the adjunct and tissue are captured within thefired staple, the adjunct can apply a stress that can withstand thepressure of circulating blood through tissue. High blood pressure istypically considered 210 mmHg, and therefore it would be desirable forthe adjunct to apply a stress to the tissue that is equal to or greaterthan 210 mmHg (e.g., 3 g/mm²) for a predetermined time period (e.g., 3days). As such, in certain embodiments, the adjunct can be configured toapply a stress of at least about 3 g/mm² to the captured tissue for atleast 3 days. The adjunct is in a tissue deployed state when the adjunctis stapled to tissue in vivo. In one embodiment, the applied stress canbe about 3 g/mm². In another embodiment, the applied stress can begreater than 3 g/mm². In yet another embodiment, the stress can be atleast about 3 g/mm² and applied to the captured tissue for more than 3days. For example, in one embodiment, the stress can be at least about 3g/mm² and applied to captured tissue for about 3 days to 5 days.

In order to design an adjunct that is configured to apply a stress of atleast about 3 g/mm² to the captured tissue for a predetermined time, onecan use the principles of Hooke's law (F=kD). For example, when theforce (stress) to be applied to the captured tissue is known, one candesign an adjunct to have a stiffness (k). The stiffness can be set bytuning the geometry of the adjunct (e.g., the diameter of the strutsand/or the interconnectivity of the struts, e.g., angles and spacebetween the struts). Further, one can design the adjunct to have amaximum amount of compression displacement for a minimum thickness oftissue, e.g., 1 mm, and therefore the length of displacement D can bethe combination of a minimum thickness of tissue, e.g., 1 mm, plus athickness of the adjunct when stapled to tissue for a given max stapleheight, e.g., 2.75 mm. By way of example, in one embodiment, an adjunctcan be structured to have a height that is greater than a maximum formedstapled height of 2.75 mm and to compress to a height of 1.75 mm whenstapled to tissue having a minimum thickness of 1 mm. Therefore, theadjunct can vary in compressibility to maintain a constant length ofdisplacement D such that the stiffness (k) and total thickness (D) ofcaptured tissue and adjunct can apply a stress of 3 g/mm² to thecaptured tissue. It should be noted a person of ordinary skill in theart will appreciate that the foregoing formula can be modified to takeinto account variations in temperatures, e.g., when the adjunct isbrought from room temperature to body temperature after implantation.

Additionally, the adjunct can be further developed to provide asubstantially continuous stress to the captured tissue (e.g., 3 g/mm²)for a predetermined time (e.g., 3 days). To achieve this, one would needto take into account the degradation rate of the materials of theadjunct and the rate of tissue ingrowth within the adjunct whendesigning the adjunct. In doing so, one can design an adjunct such thatthe stiffness of the adjunct and/or the total thickness of the capturedtissue and adjunct do not vary in a way that could effect an appliedstress that is less than 3 g/mm².

An adjunct is stapled to tissue under various stapling conditions (e.g.,tissue thickness, height of formed staple, intra-tissue pressure).Depending on the stapling condition, one can determine an effectiveamount of stress that the adjunct needs to be able to apply to thetissue to prevent tissue tearing and leakage. For example, in oneembodiment, an effective amount of stress is at least about 3 g/mm². Inorder for the adjunct to provide an effective amount of stress to thetissue, the adjunct can be designed to effectively compensate for thevarious stapling conditions. As such, the geometry of the adjunct can betailored to assume different compressed heights when stapled to tissue.As there is a finite range of intra-tissue pressures, tissuethicknesses, and formed staple heights, one can determine appropriategeometric structures for the adjunct that can be effective in applying asubstantially continuous desired stress to the tissue (e.g., 3 g/mm²)when stapled thereto for a given amount of time (e.g., at least 3 days)over a range of stapling conditions. That is, as described in moredetail below, the present adjuncts are formed of compressible materialsand geometrically configured so as to allow the adjunct to compress tovarious heights in predetermined planes when stapled to tissue. Further,this varied response by the adjunct can also allow the adjunct tomaintain its application of a continuous desired stress to the tissuewhen exposed to fluctuations in intra-tissue pressure that can occurwhen the adjunct is stapled to tissue (e.g., a spike in blood pressure).

The adjuncts can be manufactured by additive manufacturing, also knownas three-dimensional printing or 3D printing. 3D printing is ahigh-speed additive manufacturing technology that can deposit varioustypes of materials in a printer-like fashion. That is, 3D printing isachieved by laying down successive layers of material to form shapes. Toprint, the printer reads the model design from a digital file and laysdown successive layers of material to build a series of cross sections.These layers, as decided by the model, are joined or automatically fuseto create the final shape. This technique allows for the ability tocreate various shapes or geometric features with control and precision.Non-limiting examples of suitable 3D printing processes, also known asadditive manufacturing, as classified by ASTM committee 42 include VATphotopolymerication (e.g., stereolithography) in which liquidphotopolymer in a vat is selectively cured by light activatedpolymerization; material jetting in which droplets of build material areselectively deposited; binder jetting in which a liquid bonding agent isselectively deposited to join powder materials; powder bed diffusion(e.g., selective laser sintering) in which thermal energy selectivelyfuses regions of a powder bed; direct energy deposition in which focusedthermal energy is used to fuse materials by melting as they are beingdeposited; direct energy deposition in which focused thermal energy isused to fuse materials by melting as they are being deposited; materialextrusion (e.g., fused deposition modeling) in which material isselectively dispensed through a nozzle or orifice; and sheet laminationin which sheets of material are bonded to form an object.

For example, in some embodiments, the method can include scanning a beamto melt a plurality of layers of powder to form a compressible,bioabsorbable adjunct having an elongate body with a tissue-contactingsurface, a cartridge-contacting surface that is opposite thetissue-contacting surface, and a plurality of struts forming repeatinggeometric units that extend between the tissue-contacting andcartridge-contacting surfaces. In one embodiment, the method can alsoinclude coating the adjunct with one or more anti-microbial agents.

The adjunct can be formed from one or more matrices. In certainembodiments, the one or more matrices can be in the form of aparticulate matrix. In such instances, each particulate matrix can beformed of fused particles (e.g., fused bioabsorbable polymer particles).

In general, each matrix can be formed of at least one fused polymer. Theat least one fused polymer can be selected so as to impart a desiredcompressibility to the adjunct. For example, in one embodiment, thematrix includes a fused polymer, whereas in other embodiments, thematrix can include two or more fused polymers that are different.Alternatively, or additionally, where the adjunct includes two or morematrices, each matrix can be formed of the same fused polymer ordifferent fused polymers relative to each other. For example, a firstmatrix can include a first fused polymer and a second matrix can includea second fused polymer that is either more or less flexible than thefirst fused polymer. In this way, the fused polymers can provide theadjunct with varying flexibility. Further, the fused polymers can havediffering degradation rates, such that the compressibility of theadjunct can be tailored to vary over time as function of the degradationrates.

While various types of materials can be used, in some embodiments, theat least one fused polymer is a bioabsorbable polymer. Non-limitingexamples of suitable bioabsorbable polymers include thermoplasticabsorbable polyurethane, ultraviolet curable bioabsorbable polyurethane,poly(lactic acid) (PLA), polycaprolactone (PCL), polyglycolide,polydioxanone (PDS), poly(lactic-co-glycolic acid) (PLGA), polyglycolicacid, trimethylene carbonate, glycolide, dioxanone, polyester, anycopolymers thereof, or any combinations thereof. Additional non-limitingexamples of suitable bioabsorbable polymers include macromers withacrylate or methacrylate end group modified three-armed hydroxylterminated PCL or Poly (DL-lactide), PLA-PEG orpoly(trimethylenecarbonate), PEG dimethyl or trimethyl acrylate ormethacrylate, polypropylene fumarate, L-lactide/caprolactone copolymers,PLGA polymers infiltrated with collagen, PCL-tricalcium phosphate (TCP),PLGA-TCP copolymers coated with Hyaluronic acid, PCL-PLGA-TCP, PLGA-PCLcopolymers, PDS polymers and copolymers, PCL polymer and Hyaluronicacid, PCL and Beta-Tricalcium phosphate with collagen coating, polyvinylalcohol, calcium phosphate/poly(hydroxybutyrate-co-valerate), andcalcium hydroxyapatite/poly-L-lactide.

For example, in some embodiments, the adjunct can be formed of variouscomponents each being formed of a matrix that includes at least onefused bioabsorbable polymer. In some embodiments, the adjunct can have afirst component formed from a first matrix of at least one fusedbioabsorbable polymer (e.g., polyglactin or polydioxanone) and a secondcomponent formed from a second matrix that includes at least one fusedbioabsorbable polymer (e.g., a polycaprolactone copolymer). The at leastone fused bioabsorbable polymer for each matrix can include at least twodifferent bioabsorbable polymers. In one embodiment, the first componentcan have a first color and the second component can have a second colorthat differs from the first color.

In some embodiments, the adjunct can be drug eluting. For example, oneor more components of the adjunct can include a composition having apharmaceutically active agent. The composition may release atherapeutically effective amount of the pharmaceutically active agent.In various embodiments, the pharmaceutically active agent can bereleased as the adjunct is desorbed/absorbed. In various embodiments,the pharmaceutically active agent may be released into fluid, such as,for example, blood, passing over or through the adjunct. Non-limitingexamples of pharmaceutically active agents include haemostatic agentsand drugs, such as, for example, fibrin, thrombin, and oxidizedregenerated cellulose (ORC); anti-inflammatory drugs, such as, forexample, diclofenac, aspirin, naproxen, sulindac, and hydrocortisone;antibiotic and antimicrobial drug or agents, such as, for example,triclosan, ionic silver, ampicillin, gentamicin, polymyxin B, andchloramphenicol; and anticancer agents, such as, for example, cisplatin,mitomycin, and adriamycin.

The adjunct can also include an external coating. The coating may bepart of the 3D printing process or secondarily applied to the adjunct.For example, in some implementations, the adjunct can be partially orcompletely coated with antimicrobial agents. Non-limiting examples ofsuitable anti-microbial agents include triclosan, chlorhexidine, silverformulations (like nano-crystalline silver), lauric arginate ethyl ester(LAE), octenidine, polyhexamethylene biguanide (PHMB), taurolidine;lactic acid, citric acid, acetic acid, and their salts.

The adjunct, or any component thereof, can be at least partially coatedwith a bioabsorbable polymer that is different than the at least onefused bioabsorbable polymer of the adjunct. In this way, one or moreproperties of the adjunct can be varied from the properties of its basematerial(s) (e.g., fused bioabsorbable polymer(s)). For example, theadjunct can be coated with bioabsorbable polymer(s) that improve(s)structural stability. Alternatively, or in addition to, the adjunct canbe coated with a bioabsorbable polymer having a slower degradation ratecompared to the degradation rate of the at least one fused bioabsorbablepolymer of the adjunct. In this way, the longevity of the adjunct can beincreased without sacrificing the desired compressibility of the adjunctprovided at least in part by the at least one fused bioabsorbablepolymer.

The adjuncts can have a variety of configurations. In general, theadjuncts can include a tissue-contacting surface, an oppositebody-contacting surface (e.g., a cartridge-contacting layer), and anelongate body positioned therebetween (structural layer). Thetissue-contacting and cartridge-contacting surfaces can, in certainembodiments, have a structure that differs from the structural layer, soas to form tissue-contacting and cartridge-contacting layers. In someembodiments, the elongate body is formed of multiple struts. The strutscan have various configurations, and in certain exemplary embodimentsthe struts can form interconnected repeating geometric units.

In some embodiments, the tissue-contacting layer can include a pluralityof surface features thereon that are configured to engage tissue locatedbetween the adjunct and the anvil so as to substantially prevent slidingmovement of the tissue relative to the adjunct during stapling. Thesesurface features can also be configured to minimize sliding movement ofthe adjunct relative to the tissue when the adjunct is stapled thereto.These surface features can have a variety of configurations. Forexample, the surface features can extend from the tissue-contactingsurface at a distance from about 0.007 inches to 0.015 inches.

Further, in some embodiments, these surface features can extend in adirection that is substantially lateral to a longitudinal axis (L) of abody, like cartridge body 606 in FIG. 6. In another embodiment, at leasta portion of the surface features can include a plurality of ridges anda plurality of grooves defined between the plurality of ridges. In yetanother embodiment, these surface features can include a plurality oftreads extending in a direction that is at least of upwardly from abody, inwardly toward a central groove, and distally toward a second endof the body. Additional details on anti-slip features that are in theform of ridges and grooves or in the form of treads can be found in U.S.Publication No. 2015/0034696, which is incorporated by reference hereinin its entirety.

In some embodiments, the plurality of surface features can be configuredto pull tissue in opposite directions, and therefore provide acounter-resistance (e.g., lateral bias) to prevent the tissue fromsliding during stapling. For example, the tissue-contacting layer caninclude a first plurality of surface features that can extend in a firstdirection and a second plurality of surface features that can extend ina second direction that is different than the first direction. As aresult, the first and second plurality of surface features can createtension between the surface features that actively prevent motion of thetissue in at least one direction. In one embodiment, the first pluralityof surface features can extend in a first direction and the secondplurality of surface features can extend in an opposite seconddirection. In such instances, these surface features can be configuredto pull tissue in opposite directions simultaneously.

A counter resistance can also be created by surface bowing. For example,the tissue-contacting layer, or in the alternative, for example, theentire adjunct, can be designed to have a resilient convex shape, andthe surface features can extend radially outward from thetissue-contacting layer. In use, as the anvil of the surgical staplermoves from an open to a closed position, as discussed above, thetissue-contacting layer can deform (e.g., compress to a substantiallystraight configuration), and the surface features, now extendingsubstantially vertically outward from the tissue-contacting layer,engage tissue. As the anvil returns to its open position, thetissue-contacting layer returns to its convex shape creating a surfacetension between the surface features that causes the engaged tissue tobe pulled in opposite directions simultaneously.

On the other hand, in certain embodiments, it can be desirable to havethe tissue slide in a predefined plane during stapling. As such, in someembodiments, the tissue-contacting layer can include surface featuresthat can be designed to promote slippage (e.g., a sliding movement) ofthe tissue relative to the adjunct in a first predetermined directionand to limit movement in a second direction that is different than thefirst direction. Alternatively, or additionally, the tissue-contactinglayer can be coated with a material to increase lubricity (e.g., sodiumstearate or lauric arginate ethyl ester).

As discussed above, the adjunct is positioned atop a body, likecartridge body 606 (FIG. 6). Prior to and during stapling, securement ofthe adjunct to the body can be enhanced. For example, thebody-contacting layer (e.g., a cartridge-contacting layer) can includesurface features that are configured to engage the body so as tosubstantially prevent sliding of the adjunct relative to the body. Thesesurface features can have a variety of configurations. For example inembodiments where the body includes attachment features, thebody-contacting layer can have surface features that are in the form ofrecesses that are configured to receive these attachment features. Otherattachments features will be discussed in more detail below.

As indicated above, the elongated body can be formed of a plurality ofstruts. These struts can form repeating geometric units interconnectedto one another. As discussed in more detail below, the plurality ofstruts and/or the array of repeating units can be structurallyconfigured to impart a varying compressibility to the adjunct, and thusthe adjunct can have a variable stiffness profile. For example, theadjunct can have a first stiffness when compressed a first amount and asecond stiffness when compressed a second amount. The second amount canbe greater than the first amount or vice versa. Thus, the stiffness ofthe adjunct can vary as a function of compression. As discussed in moredetail below, the greater the amount of compression, the greater thestiffness of the adjunct. Accordingly, a single adjunct can be tailoredto provide a varied response that ensures a minimum amount of stress isapplied to the tissue (e.g., 3 g/mm²) for at least a predetermined time(e.g., 3 days) under various stapling conditions (e.g., tissuethickness, height of formed staple, intra-tissue pressure). Further,this varied response by the adjunct can also desirably maintain theminimum amount of applied stress (e.g., 3 g/mm²) when the adjunct isstapled to tissue and exposed to fluctuations in intra-tissue pressure.

These struts can be designed in various configurations. For example,these struts can produce lattice or truss-like structures as shown inFIGS. 8A-9C and 11A-15, spiral shaped structures as shown in FIG. 16, orcolumns as shown in FIGS. 17-19.

The geometry of the struts themselves, as well as the geometry of therepeating units formed therefrom, can control movement of the adjunct invarious planes. For example, the interconnectivity of the struts cancreate geometric units that can be configured to allow the adjunct tocompress in a first predetermined direction and to limit movement in asecond direction that differs from the first direction. As discussed inmore detail below, in some embodiments, the second direction can betransverse to the first predetermined direction. Alternatively, or inaddition to, the geometric units can be configured to limit rotationalmovement of the adjunct about an axis that is perpendicular to the firstpredetermined direction.

In some embodiments, a strut can have a substantially uniformcross-section, whereas in other embodiments, the strut can have avarying cross-section. Additionally, the material of the strut can alsoplay a role in defining movement of the adjunct in predetermined planes.

FIGS. 8A-9C and 11A-19 illustrate various exemplary adjuncts thatinclude a tissue-contacting surface, a cartridge-contacting surface thatis opposite the tissue-contacting surface, and an elongate body formedof struts positioned therebetween. Each exemplary adjunct is illustratedin partial form (e.g., not in full-length), and therefore a person ofordinary skill in the art will appreciate that the adjunct can be longerin length, i.e., along its longitudinal axis L as identified in eachembodiment. The length can vary based on a length of the staplecartridge. Further, each exemplary adjunct is configured to bepositioned atop a cartridge body such that the longitudinal axis L ofeach adjunct is aligned with and extends along the longitudinal axis(L_(C)) of the cartridge body. Each of these adjuncts can be formed fromone or more matrices that include at least one fused bioabsorbablepolymer. These adjuncts are structured so as to compress when exposed tocompressive forces (e.g., stress or load). As discussed in furtherdetail below, these adjuncts are also designed to promote both tissueand cellular ingrowth.

FIGS. 8A-8B illustrate an exemplary embodiment of an adjunct 800 havinga tissue-contacting surface 802, an opposite cartridge-contactingsurface 804, and an elongate body 806. While it is contemplated that thetissue-contacting surface 802, the cartridge-contacting surface 804, andthe elongate body 806 can each be formed from different materials, inthis illustrated embodiment, they are formed of the same fusedbioabsorbable polymer. That is, the adjunct 800 is formed of a matrix ofthe same fused bioabsorbable polymer.

As shown in FIG. 8A, the elongate body 806 includes a planar array 808of repeating units 810 interconnected to one another at joints or nodes814. The repeating units 810 are each formed of a plurality ofinterconnected struts 816 that each have a first portion 818 and asecond portion 820. Some of the struts 816 can also include a thirdportion 821 that extends from their respective second portion andinterconnect to one another to form the joints or nodes 814. Asdiscussed in more detail below, the adjunct 800 can exhibit varyingstiffness and movement based on the amount and direction of stressapplied thereto during use. Thus, the adjunct has a variable stiffnessprofile such that when the adjunct is stapled to tissue, the adjunct canbe configured to apply a stress at or above a minimum stress thresholdfor a predetermined time (e.g., a stress of 3 g/mm² for at 3 days).

Further, as shown, the elongate body 806 includes a first planar array808 of struts, and additional planar arrays 808 _(N) positioned parallelto one another and to planar array 808 (e.g., extending in thex-direction). In each array 808, 808 _(N), the struts 816 aresubstantially planar and extend co-planar with one another in arespective plane. Further, while each array 808, 808 _(N) can have avariety of configurations, in this illustrated embodiment, each array808, 808 _(N) is substantially symmetric about a mid-plane. That is,each array 808, 808 _(N) has two substantially identical, rows 824 a,824 b of repeating units 810.

While the struts 816 can have a variety of configurations, in thisillustrated embodiment, each strut 816 has a generally elongate planarconfiguration, with the first portion 818 of each strut 816 having anarrower width than a width section of the second portion 820. As aresult, the struts 816 are wider in the middle, preferably along amajority of the length, and narrower at the ends. Alternatively, thefirst portion 818 can have a cross section that is equal to or greaterthat the cross section of the second portion 820. Further, as shown inFIG. 8B, the second portion 820 of each strut 816 can have asubstantially rectangular cross-sectional shape. It should be noted thatother cross-sectional shapes of the struts, and portions thereof, arealso contemplated herein. The cross-sectional shapes of the struts canbe used to limit movement of the adjunct in certain directions.

In FIG. 8A, the struts 816 are interconnected to one another at an endof their first portion 818 to form joints or nodes 822. In theillustrated embodiment, the struts 816 and the joints or nodes 822 canbe formed of the same material. Thus, to enhance the compression of theadjunct 800 under stress, the cross-section of the first portion 818,also referred to as a neck down region, can flex as described in moredetail below. Further, the third portion 821 of the respective struts816 is similarly structured like the first portion 818 of the struts816, and therefore this third portion 821, also referred to as a neckdown region, can also flex as in more detail below.

The material of the joints or nodes 822 relative to the struts 816(e.g., more or less flexible) can control, in part, the amount and/ordirection at which the adjunct 800 moves under stress during use.Likewise, the material of the joints or nodes 814 can control, in part,the amount and/or direction at which the adjunct 800 moves under stressduring use. The joints or nodes 814, 822 can be any suitable shape. Forexample, in certain embodiments, the joints or nodes 814, 822 can be inthe form of a ball-shaped feature. In other embodiments the joints ornodes 814, 822 can take the form of other geometric shapes.

The struts 816 can be interconnected to each other at various angles.For example, in this illustrated embodiment, the struts 816 intersect atabout 90 degree angles relative to adjacent struts 816. In otherembodiments, the struts 816 can intersect at angles in a range of about40 degrees to 130 degrees. In another embodiment, the struts 816 canintersect at angles in a range of about 10 degrees to 90 degrees. Theangles at which the struts 816 connect to each other can control, atleast in part, the manner and the amount in which the adjunct 800responds under stress. That is, the movement and stiffness of theadjunct 800 can be, at least in part, a function of these angles.

As mentioned above, the first portion 818 (and the third portion 821where present) of each strut 816 can act as a flexible region for theadjunct (e.g., a deflection point). The first portion 818 of each strutprovides each repeating unit 810 with one or more bend zones, asillustrated in FIGS. 9A-9C. That is, these neck down regions allow thestruts 816 to bend about or adjacent to the joints or nodes 822 when theadjunct 800 is under stress, and therefore the repeating units 810 canpartially or fully collapse upon themselves. Similarly, the neck downregions that form the third portion 821 allow the repeating units tobend about or adjacent to the joints or nodes 814 when the adjunct isunder stress. The compressibility of the adjunct 800 can therefore varybased on different amounts and directions of applied stress. Thisvariation in compressibility can be desirable, for example, when theadjunct is stapled to tissue and exposed to fluctuations in intra-tissuepressure.

FIGS. 9A-9C illustrate the compression behavior of one repeating unit810 of adjunct 800 as described herein under different stresses. Inparticular, the repeating unit 810 is shown in an pre-compressed(undeformed) state in FIG. 9A, a first compressed state under a firststress (S₁) in FIG. 9B, and a second compressed state (C) under a secondstress (S₂) in FIG. 9C. As such, the repeating unit 810, and thusadjunct 800, has a variable stiffness profile under different stresses.A person of ordinary skill in the art will appreciate that the adjunctcan have a variety of deployed heights throughout its use, and that thedeployed heights are a function of, at least in part, the particularstresses that are applied to the adjunct throughout its use.

As shown in FIGS. 9A-9B, when the repeating unit 810, and thus adjunct800 in FIG. 8A, is under a first stress S₁, the first portion 818 (e.g.,the neck down region) of each strut 816 can bend about the joint or node822. This allows the repeating unit 810 to compress from apre-compressed state (FIG. 9A) to a first compressed state (FIG. 9B),and thus adjunct 800 from a pre-compressed height to a first deployedheight. Further, depending on the amount of stress applied to theadjunct, the second portion 820 of adjacent struts 816 can come intocontact with each other. This is illustrated in FIG. 9B. In suchinstances, the first portion 818 of each strut 816 has therefore reacheda maximum deflection point creating a greater stiffness resistancewithin the repeating unit 810. This is because the stiffness of therepeating unit 810, and thus the adjunct 800, increases as the adjunct800 compresses. FIG. 10 is an exemplary graph representation of therelationship between compression and stiffness of an adjunct. Thus, anyfurther compression of the repeating 810, and thus the adjunct 800 wouldrequire an additional applied stress.

In circumstances where a greater stress (e.g., second stress, S₂) isapplied to the repeating unit 810, and thus adjunct 800 in FIG. 8A, theincrease in stiffness resistance can be overcome. To achieve this, thestruts 816 can be configured such that when additional stress isapplied, the struts 816 can further bend about the joint or node 822. Asshown in FIG. 9C, this further bending can cause the struts 816 tofurther expand outward in a direction lateral (L) to the direction ofapplied stress, whereby causing the second portions 820 of adjacentstruts 816 to come into further contact with each other. As a result,this allows the repeating unit 810 to compress to a second compressedstate (FIG. 9C), and thus adjunct 800 to a second deployed height.

In some embodiments, the adjunct can include additional components thatcan prevent movement of tissue that is stapled to the adjunct. Forexample, FIGS. 11A-11B illustrate an exemplary adjunct 1100 thatincludes a plurality of surface features 1128 defined within thetissue-contacting layer 1102. As described in more detail below, thesurface features 1128 can prevent slidable movement of the adjunctrelative to tissue stapled to the adjunct. In one embodiment, at least aportion of the surface features 1128 can prevent lateral sliding of theadjunct 1100 relative to the tissue. Alternatively, or in addition to,at least a portion of the surface features 1128 can prevent longitudinalsliding of the adjunct 1100 relative to the tissue.

The illustrated exemplary adjunct 1100 includes a tissue-contactinglayer 1102 and an opposite cartridge-contacting layer 1104. The adjunct1100 also includes an elongate body 1106 having a plurality of struts1116 extending between the tissue-contacting layer 1102 and thecartridge-contacting layer 1104. As shown, the tissue-contacting layer1102 includes a plurality of surface features 1128 defined therein.These surface features 1128 have a grid-like pattern with a first series1128 a extending longitudinally (e.g., parallel to the longitudinal axisof the adjunct) and a second series 1128 b extending laterally (e.g.,traverse to the longitudinal axis of the adjunct). Each surface feature1128 a, 1128 b can have a triangular profile, or at least two surfacesthat are angled relative to one another and that come together to forman edge so as to penetrate into and engage tissue. These edgescollectively can define the outer-most surface of the tissue-contactinglayer 1102. These surface features 1128 a, 1128 b can engage tissue whenthe tissue is compressed into the tissue-contacting layer 1102 as aresult of the adjunct being stapled to tissue. The orientation of theedges of the first series 1128 a can prevent lateral sliding of theadjunct relative to the tissue and the orientation of the edges of thesecond series 1128 b can prevent longitudinal sliding of the adjunct1100 relative to the tissue. Further, the tissue-contacting layer 1102includes a plurality of openings 1144 that are formed between thesesurface features 1128. In this way, the plurality of openings 1144 canreceive tissue therein when the adjunct is stapled to tissue to allowthe surface features 1128 to engage the tissue.

While the plurality of struts 1116 can be interconnected to form avariety of configurations, in this illustrated embodiment, the pluralityof struts 1116 form repeating X patterns. In particular, the pluralityof struts 1116 form repeating cubic units. Each cubic unit includes atop surface 1130 and an opposing bottom surface 1132. In thisillustrated embodiment, the top and bottom surfaces 1130, 1132 aresubstantially identical. The cubit unit also includes four side surfaces1134 extending between and connecting the top and bottom surfaces 1130,1132. In this illustrated embodiment the side surfaces 1134 aresubstantially identical. For clarity, not all surfaces of eachillustrated cubit unit are identified in FIGS. 11A-11B. The sidesurfaces 1134 can have a variety of shapes, for example, as shown eachside surface 1134 has an X shape that extends from the top to the bottomsurfaces 1130, 1132. As such, the first end of each strut 1116terminates at the tissue-contacting layer 1102 and the second end ofeach strut 1116 terminates at the cartridge-contacting layer 1104. EachX can be formed by two elongated, generally planar struts that intersectat a mid-portion. Further, each repeating cubic unit can also include aninternal strut that extends between two opposite side surfaces 1134 ofthe cubic unit to form an inner connectivity feature 1138. As shown, theinner connectivity feature 1138 can extend from the top 1134 a of oneside surface 1134 to the bottom 1134 b of an opposing side surface 1134.As further shown, the inner connectivity features 1138 can extend inalternating directions between adjacent cubic units. For example, asshown in FIG. 11B, a first inner connectivity feature 1138 can have anupper end 1138 a that extends from the top 1134 a of one side surface1134 to a lower end 1138 b at the bottom 1134 b of the opposite sidesurface 1134, and the adjacent cubic unit can have a second innerconnectivity feature 1138 with a lower end 1138 c that extends from thesame bottom 1134 b of the side surface 1134 to an upper end 1138 d at atop 1134 c of an opposite side surface 1134. The inner connectivityfeatures 1138 can provide the adjunct 1100 with a geometry that canpromote predetermined directional movement of the adjunct 1100 underapplied stress. For example, in one embodiment, the inner connectivityfeatures 1138 can substantially prevent shearing of the adjunct 1100under applied stress.

While each strut, as well as the interconnectivity features 1138, canhave a variety of configurations, in this illustrated embodiment, thestruts 1116 and the interconnectivity features 1138 are each in the formof a beam or column having a width (W) that is greater than a depth (D)such that each strut/interconnectivity feature is limited to bending ina predetermined direction, i.e., in and out of the plane extending alongthe width (W). Further, the struts 1116 and the interconnectivityfeatures 1138 can each include at least one opening 1140 extendingtherethrough to facilitate bending in a predetermined direction. Forclarity purposes, not all openings 1140 extending through each strut1116 and the interconnectivity features 1138 are identified in FIGS.11A-11B. These openings 1140 can a variety of shapes, for example, asshown, these openings 1140 are diamond shaped. It is also contemplatedthat the shape of the openings 1140 can vary among struts. The openings1140 can also be aligned throughout the adjunct. For example, openingsextending through opposite sidewalls spaced longitudinally along thelength of the adjunct in adjacent cubic units can be alignedlongitudinally, and similarly openings extending through oppositesidewalls spaced laterally along the width of the adjunct in adjacentcubic units can be aligned laterally.

Alternatively, or additionally, the adjunct can include linking membersthat connect at least a portion of the joints or nodes to each other tothereby increase the stiffness of the adjunct. That is, the linkingmembers can be incorporated into the adjunct so as to prevent movement(e.g., splaying) of the adjunct in the planes in which the linkingmembers extend.

For example, FIGS. 12A-12B illustrate an exemplary embodiment of anadjunct 1200 having linking members 1246. In particular, the adjunct1200 includes an elongate body 1206 formed of a plurality of struts 1216that are interconnected at joints or nodes 1222. The elongate body 1206has a tissue-contacting surface 1202 and an oppositecartridge-contacting surface 1204. As shown, at least a portion of thesejoints or nodes 1222 are interconnected to each other by linking members1246. In this illustrated embodiment, the linking members 1246 extend ina first direction (e.g., the y-direction as shown in FIG. 12) and thestruts 1216 extend in a second direction that is different than thefirst direction (e.g., a transverse direction, such as about 45 degreesrelative to the y-direction as shown in FIG. 12). Thus, the position ofthe linking members 1246 relative to the struts 1216 can provide theadjunct 1200 with a geometry that can be configured to prevent movementof the adjunct 1200 in at least in one direction (e.g., a directionparallel to the direction in which the linking members 1246 extend).

In some embodiments, the joints or nodes can be formed of material thatdiffers from the material of the struts. For example, the material ofthe joints or nodes can be more flexible than the material of thestruts, thereby increasing the compressibility of the adjunct. Further,the more flexible joints or nodes can also allow the adjunct to compresswithout substantially shearing. This is because the more flexible jointsor nodes provide preferential bending zones for the adjunct, therebydecreasing the stiffness of the adjunct. In one embodiment, the jointsor nodes can be formed of a polycaprolactone copolymer and the strutscan be formed of polyglactin or polydioxanone.

FIGS. 13A-13B illustrate another exemplary embodiment of an adjunct 1300that includes repeating units 1310 interconnected to one another atjoints or nodes 1314. The repeating units 1310 are each formed of aplurality of struts 1316, e.g., four struts, that interconnect at jointsor nodes 1322. Aside from the differences described in detail below, theadjunct 1300 can be similar to adjunct 800 (FIG. 8A) and is thereforenot described in detail herein. In this illustrated embodiment, thejoints or nodes 1314, 1322 are formed of a different material than thematerial of the struts 1316. The material of the joints or nodes 1314,1322 can be more flexible than the material of the struts 1316. Asshown, each joint or node 1314, 1322 can be in the form of a rod 1348that extends across all arrays 1308, 1308 _(N) in a direction that isgenerally perpendicular to the plane in which the struts extend (e.g.,the rods can extend in the x-direction as shown in FIGS. 13A-13B). Thatis, when the adjunct 1300 is attached to a cartridge body, the rods 1348can extend laterally relative to the longitudinal axis of a cartridgebody, like cartridge body 606 in FIG. 6.

In some embodiments, as shown in FIGS. 13A-13B, the ends of the firstportions 1318 of the struts 1316 can also be directly connected to eachother within the joints or nodes 1322. Alternatively, or additionally,the ends of the third portions 1321 of the struts 816 can also bedirectly connected to each other within the joints or nodes 1314. Thisdirect connection can help prevent the struts 1316 from pulling out ofthe joints or nodes 1322 as the struts 1316 bend when the adjunct 1300is under stress. As a result of this direct connection, the bending ofone strut can also influence the bending of another. Further, ascompared to joints or nodes 822 in FIG. 8A, these joints or nodes 1322can be more flexible, thus more compliant, and the adjunct 1300 cantherefore compress more easily compared to adjunct 800. As such, underthe same given stress, the adjunct 1300 will achieve a greaterdisplacement (i.e., compress to a lower deployed height) as compared toadjunct 800 in FIG. 8A.

Alternatively, the struts can be unconnected relative to each otherwithin the joints or nodes, for example, as shown in FIG. 14. Forsimplicity purposes only, FIG. 14 illustrates a single repeating unit1400. In this illustrated embodiment, the struts 1416 do not directlyconnect to one other within the joint or node 1422. As a result, thebending of one strut can occur independent of the bending of anotherstrut. To prevent the struts 1416 from pulling out of the joint or node1422 when the struts 1416 bend thereabout, each strut 1416 can have anend shape 1450 configured to maintain its connection to the joint ornode 1422. Further, as compared to joints or nodes 1322 in FIGS.13A-13B, this joint or node 1422 can be more flexible, and thus morecompliant, and therefore an adjunct formed of various repeating units1400 can compress more easily under a given stress. That is, under thesame given stress, an adjunct with this illustrated strut and joint ornode configuration can achieve a greater displacement (i.e., compress toa lower height) as compared to adjunct 800 in FIGS. 13-13A.

In some embodiments, the adjunct can also include at least one stopelement that is configured to limit the amount of compression of theadjunct. FIG. 15 illustrates an exemplary embodiment of an adjunct 1500having at least one stop element 1552. Aside from the differencesdescribed in detail below, the adjunct 1500 can be similar to adjunct1300 (FIGS. 13A-13B) and is therefore not described in detail herein.

In FIG. 15, each strut 1516 can have a stop element 1552 extending fromor positioned adjacent to a surface of its second portion 1520. As theadjunct 1500 is compressed, the struts 1516 can bend about the joint ornodes 1514, 1522 until the stop elements 1552 come into contact witheach other. Once these stop elements 1552 abut one another, any furtherbending of the struts 1516 will be inhibited. That is, these stopelements 1552 act as deflection stops that allow the adjunct 1500 tocompress under a given stress to a first deployed height at a firststiffness. Upon reaching the first compressed height, the stop elements1552 bottom out and inhibit further deflection of the struts 1516, andthus further compression of the adjunct 1500. Once the stop elements1552 bottom out, a greater amount of stress needs to be applied toeffect further bending of the struts 1516 about the joints or nodes1514, 1522 and thus further compression of the adjunct 1500.

It should be noted that while various stop elements 1552 are shown inFIG. 15, it is contemplated herein that fewer or additional stopelements can be included throughout the adjunct 1500. Further, theshape, size, and location of the stop elements 1552 are not limited bythis illustrated embodiment, and therefore can vary to control thedesired amount of compression.

As mentioned above, the elongated body can include a plurality of strutsthat can have a variety of shapes. For example, FIG. 16 illustrates anexemplary adjunct 1600 having an elongate body 1606 that includes aplurality of struts 1616 that are substantially spiral-shaped. As such,each repeating geometric unit is in the form of a spiral or coil. Inthis embodiment, the elongate body 1606 is positioned between atissue-contacting layer 1602 and a cartridge-contacting layer 1604. Asshown, each layer 1602, 1604 are generally planar solid layers withopenings 1626. At least a portion of these openings 1626 are alignedwith the openings 1615 defined by each strut 1116. The thickness of eachlayer can vary. The struts 1616 are configured to have predeterminedcompressed heights to limit an amount of compression of the adjunct.Further, given their shape, these struts 1616 can be configured tofunction as a spring. Thus, similar to a spring constant, a specificstiffness can be imparted to each strut 1616 based on its shape. Thus,the compressibility of the adjunct 1600 can also be dependent on thespecific stiffness of each strut 1616, which is dependent on both thematerial and shape of the strut 1616.

As shown in FIGS. 8A, 11A-13B, and 15-16, each adjunct 800, 1100, 1200,1300, 1500, 1600 can include openings 826, 1140, 1144, 1226, 1326, 1526,1626. These openings can be configured to promote cell ingrowth withineach adjunct. The openings can define a void content of the adjunct. Insome embodiments, the void content can be from about 15% to 95%, whereasin other embodiments, the void content can be from about 75% to 90%. Asused herein, “openings” is used synonymously with “voids”. Further, theadjunct can have a surface area to volume ratio of about 1:100 to 1:5.In some embodiment, the adjunct can have a surface area to volume ratioof about 1:10.

The openings can also be located within various components of theadjuncts. Each opening can have a dimension extending at least partiallythrough the component. In certain embodiments, as shown in FIGS. 8A,11A-13B, and 15-16, the openings 826, 1144, 1226, 1326, 1526, 1615, 1626can be present within the tissue-contacting surface or layer, thecartridge contacting surface or layer, and/or the elongated body. Inthese illustrated embodiments, these openings extend completely throughits respective component. Within the elongate body, these openings canbe defined by the interconnected struts. Further, these openings canalso be interconnected throughout the adjunct to thereby form asubstantially continuous network of openings or channels. Further, asshown in FIGS. 11A-11B, openings 1140 can also be present within innerconnectivity features 1138.

The openings can have varying sizes and/or shapes. For example, largeropenings can allow tissue (and cells) to penetrate into the adjunctwhile smaller openings can trap cells within the adjunct to promote cellingrowth. In this way, the variable opening sizes throughout theadjuncts can promote extracellular remodeling. That is, the variableopening sizes can facilitate revascularization as well as mobility ofcells within the adjunct when the adjunct is implanted, therebyencouraging both tissue and cellular ingrowth. Further, the variableopening sizes can also facilitate extraction of byproducts and cellularwaste from the implanted adjunct, and thus the implantation site. Insome embodiments, the openings are substantially circular-shaped.

In embodiments where openings are located within the tissue-contactingsurface or layer and the elongate body, such as in FIGS. 8A, 11A-13B,and 15-16, the openings can each have a diameter that is about 70% to170% of a diameter of a staple leg of a staple, like staple 406 in FIGS.4-5. The openings within the tissue-contacting surface and within theelongate body can have a variety of sizes. For example, in someembodiments, the openings in the tissue-contacting surface can each havea diameter in the range of about 100 μm to 1000 μm. In one embodiment,the openings in the tissue-contacting surface can each have a diameterthat is at least about 14 μm. The openings in the elongate body can eachhave a diameter in the range of about 200 μm to 610 μm or of about 400μm to 1000 μm. As used herein, “diameter” of an opening is the largestdistance between any pair of vertices of the opening.

Further, in some embodiments, the openings within the tissue-contactingsurface or layer can be configured to allow one or more portions oftissue to penetrate or compress into the tissue-contacting surface orlayer (e.g., openings 1144, 1226, 1626). In this way, as discussedabove, when the adjunct is stapled to tissue and the tissue iscompressed into the opening, slidable movement of adjunct relative tothe tissue can be substantially prevented.

In other embodiments, the adjunct can be configured to enhance stapleleg advancement through the adjunct. For example, the adjunct can haveopenings that are aligned with the advancement direction of the staplelegs into and partially through the adjunct. The openings can extendpartially or completely through the adjunct. Thus, as the staple legsadvance through the adjunct, the openings can act as a guide to minimizedamage to the staple, as well as the adjunct, as the staple passestherethrough.

In some embodiments, as shown in FIGS. 17-19, the adjunct can include aplurality of struts that are in the form of columns. For example, inFIG. 17, the columns can be substantially vertical and of varyingheights. Further, in other embodiments, as shown in FIG. 19, a first setof columns can be substantially vertical and a second set of columns canbe curved. The struts can be formed of the same or different material.In some embodiments, the adjunct can include a first plurality of strutsthat are formed of a first material and a second plurality of strutsthat are formed of a second material.

In FIG. 17, the adjunct 1700 includes a plurality of struts 1716 thatare in the form of substantially vertical columns. In particular, thesestruts 1716 extend from a cartridge-contacting layer 1704 toward, and insome instances to, the opposing tissue-contacting layer 1702. Theplurality of struts 1716 includes a first plurality of vertical struts1716 a having a first height (Y₁), a second plurality of struts 1716 bhaving a second height (Y₂) that is less than the first height (Y₁), anda third plurality of struts 1716 c having a third height (Y₃) that isless than the second height (Y₂). For simplicity, only a portion of theplurality of struts 1716 are shown in FIG. 17. While not shown, a personof ordinary skill will appreciate that the tissue- and/or cartridgecontacting layers 1702, 1704 can include openings as discussed herein.

The varying heights of these plurality of struts 1716 can provide theadjunct with varying compressibility. FIGS. 18A-18C illustrate thecompression behavior of adjunct 1700 under different stresses. Inparticular, the adjunct 1700 is shown at a pre-compressed height in FIG.18A, a first compressed height (H₁) under a first stress (S₁) in FIG.18B, and a second compressed height (H₂) under a second stress (S₂) inFIG. 18C. As shown, the first compressed height (H₁) is greater than thesecond compressed height (H₂), and therefore the first stress (S₁) isless than the second stress (S₂). A person of ordinary skill in the artwill appreciate that the adjunct can have a variety of compressedheights throughout its use, and that the compressed heights are afunction of, at least in part, the particular stresses that are appliedto the adjunct throughout its use.

As shown in FIGS. 18A-18C, as the compression of the adjunct 1700increases, the amount of stress needed to achieve such compressesincreases. This is because additional struts are engaged as the adjunct1700 compresses, thereby increasing the stiffness resistance of theadjunct 1700. For example, as shown in FIG. 18B, at a first stress S₁applied to the adjunct 1700, the first and second plurality of struts1716 a, 1716 b are engaged. In comparison, when the adjunct 1700 isunder a second stress S₂, the first, second, and third plurality ofstruts 1716 a, 1716 b, 1716 c are engaged, thereby creating a greaterstiffness resistance.

FIG. 19 illustrates another exemplary embodiment of an adjunct 1900having a plurality of struts 1916 that are in the form of substantiallyvertical columns 1916 a or curved columns 1916 b. The substantiallyvertical columns 1916 a can be configured to support the initial stressapplied to the adjunct 1900, and then deflect or buckle (e.g., atdeflection point D in FIG. 20) as the adjunct compresses. The curvedcolumns 1916 b can configured to provide approximately constantstiffness (i.e., essentially the offset of the whole curve shown in FIG.20 from the zero axis). This mechanical behavior of the struts 1916, andthus the adjunct 1900, is graphically represented in FIG. 20.

In other embodiments, the adjunct can include additional features. Thefollowing figures illustrate features that can be included on any of theadjuncts disclosed herein, and thus the specific configuration of theadjunct, i.e., the configuration of the repeating units, is not shown.FIG. 21A illustrates one embodiment of an adjunct 2100 having a channel2108 formed therein that is configured to receive a cutting element,such as a knife.

As shown in FIG. 21A, the adjunct 2100 includes a first portion 2104 anda second portion 2106, each having outer and inner edges. The inneredges 2104 a, 2106 a define a channel 2108 that extends between thefirst and second portions and along the longitudinal axis (L) of theadjunct 2100. The channel 2108 is configured to receive a cuttingmember, such as a knife. As shown in FIG. 121B, the channel 21 does notextend completely through the height of the adjunct 2100. In particular,the channel 2108 does not extend through the cartridge-contactingsurface 2110. In this way, the adjunct 2100 is configured to havesufficient structural integrity to thereby be effectively manipulatedand attached to a cartridge body, like cartridge body 2214 in FIG. 21B.In use, when the cutting member is initially fired and travels along theadjunct, the cutting member cuts through the channel, thereby separatingthe first and second portions, and thus separating the adjunct 2100 intotwo separate pieces.

Further, as shown in FIG. 21A, the adjunct 2100 includes flanges 2112that are configured to mate with a cartridge body 2214 in FIG. 21B, asfurther described below. While FIG. 21A illustrates the adjunct 2100having flanges 2112 at one side of the adjunct 2100, additional flanges2112 can be present on the opposite side of the adjunct 2100. A personskilled in the art will appreciate that the number and placement offlanges 2112 are not limited to what is shown in FIG. 21A. While theflanges 2112 can be made of a variety of materials, in someimplementations, as shown in FIG. 21A, the flanges 2112 can be anextension of the cartridge-contacting surface 2110. A person skilled inthe art will appreciate that the flanges can be formed in-line with theadjunct (e.g., as part of the 3D printing process), or in thealternative formed off-line and then secondarily applied to the adjunct.

FIG. 21B illustrates an embodiment of a staple cartridge assembly 2200.Aside from the differences described in detail below, the staplecartridge assembly 2200 can be similar to staple cartridge assembly 600(FIG. 6) and is therefore not described in detail herein. Further, forpurposes of simplicity, certain components of the staple cartridgeassembly 2200 are not illustrated in FIG. 21B.

The staple cartridge assembly 2200 includes the adjunct 2100 in FIG. 21Aattached to a cartridge body 2214. The adjunct 2100 can be attached tothe cartridge body 2214 using any suitable methods, as described in moredetail below. In this embodiment, the cartridge body 2214 includesrecessed channels 2216 that are configured to receive the flanges 2112on the adjunct such that the flanges 2112 can engage the side(s) of thecartridge body 2214. In this way, the adjunct 2100 can be more securelyattached to the cartridge body, thereby preventing undesired movement ofthe adjunct 2100 during use.

In another embodiment, as shown in FIG. 22, the adjunct 3000 can have achannel 3008 that has one or more openings 3010 extending therethrough(e.g., perforated), thereby creating at least one bridging member 3012.As such, the first and second portions 3014, 3016 of the adjunct 3000are selectively connected by the at least one bridging member 3012. Inuse, when the cutting member is initially fired and travels along theadjunct 3000, the cutting member cuts through the at least one bridgingmember 3012, thereby separating the first and second portions 3014,3016, and thus separating the adjunct 3000 into two separate pieces.

In some embodiments, the cartridge body, like cartridge body 2214 inFIG. 21B, and the adjunct, like adjunct 3000 in FIG. 22, can includecomplementary reinforcement features that can be configured to preventtearing of the adjunct outside of the channel when the cutting elementmoves through the adjunct 3000. For example, the reinforcement featuresof the cartridge body can be cylindrical recessed openings positionedproximate to the slot within the cartridge body and the reinforcementfeatures of the adjunct can be cylindrical protrusions positioned withinthe first and second portions of the adjunct proximate to the at leastone bridging member. In this way, when the adjunct is placed atop thecartridge body, these cylindrical protrusions of the adjunct will extendinto these recessed openings of the cartridge body. It is alsocontemplated that these protrusions and recessed openings can take theform of other various shapes.

The scaffolds can be applied to a cartridge body to form a staplecartridge assembly using any suitable method. For example, in someembodiments, the method can include attaching a compressible,bioabsorbable adjunct to a cartridge body of a surgical stapler. In oneembodiment, as discussed above, the attachment of the adjunct to thecartridge body can include placing a cartridge-contacting surface of theadjunct against a surface of the cartridge body so as to insert flangesof the adjunct into recessed channels of the cartridge body. In anotherembodiment, the method can also include coating a surface of thecartridge body with an adhesive prior to attaching the adjunct thereto.

The devices disclosed herein can be designed to be disposed of after asingle use, or they can be designed to be used multiple times. In eithercase, however, the device can be reconditioned for reuse after at leastone use. Reconditioning can include any combination of the steps ofdisassembly of the device, followed by cleaning or replacement ofparticular pieces and subsequent reassembly. In particular, the devicecan be disassembled, and any number of the particular pieces or parts ofthe device can be selectively replaced or removed in any combination.Upon cleaning and/or replacement of particular parts, the device can bereassembled for subsequent use either at a reconditioning facility, orby a surgical team immediately prior to a surgical procedure. Thoseskilled in the art will appreciate that reconditioning of a device canutilize a variety of techniques for disassembly, cleaning/replacement,and reassembly. Use of such techniques, and the resulting reconditioneddevice, are all within the scope of the present application.

One skilled in the art will appreciate further features and advantagesof the invention based on the above-described embodiments. Accordingly,the invention is not to be limited by what has been particularly shownand described, except as indicated by the appended claims. Allpublications and references cited herein are expressly incorporatedherein by reference in their entirety. Any patent, publication, orinformation, in whole or in part, that is said to be incorporated byreference herein is incorporated herein only to the extent that theincorporated material does not conflict with existing definitions,statements, or other disclosure material set forth in this document. Assuch the disclosure as explicitly set forth herein supersedes anyconflicting material incorporated herein by reference.

What is claimed is:
 1. A stapling assembly for use with a surgicalstapler, comprising: a body having a first end and a second end, and alongitudinal axis extending therebetween, wherein the body has a slotthat extends into and along at least a portion of the longitudinal axisand configured to receive a cutting element; and a three-dimensionalcompressible adjunct formed from a matrix comprising at least one fusedbioabsorbable polymer and configured to be releasably retained on thebody, the adjunct comprising, a first longitudinal portion having afirst plurality of struts interconnected at nodes to form a firstplurality of truss structures, a second longitudinal portion having asecond plurality of struts interconnected at nodes to form a secondplurality of truss structures, and a longitudinal channel extendingbetween the first longitudinal portion and the second longitudinalportion; and wherein the first and second longitudinal portions areconfigured to be positioned on opposite sides of the slot with thechannel extending along the slot of the body to facilitate cutting alongthe longitudinal channel as the cutting element moves through the slot.2. The stapling assembly of claim 1, wherein the channel has one or moreopenings extending therethrough.
 3. The stapling assembly of claim 1,wherein at least a portion of the channel is cut as the cutting elementdistally advances through the slot.
 4. The stapling assembly of claim 1,wherein the body further comprises a plurality of staples disposedtherein, and wherein the plurality of staples are configured to bedeployed into tissue such that the adjunct can be attached to tissue bythe plurality of staples.
 5. The stapling assembly of claim 4, whereinthe adjunct has an undeformed state in which a maximum height of theadjunct is greater than a maximum height of the plurality of staples ina formed configuration when the staples are deployed into tissue.
 6. Thestapling assembly of claim 1, wherein the adjunct is configured to applya stress of at least about 3 g/mm² to the tissue stapled thereto for atleast 3 days when the adjunct is in a tissue deployed state.
 7. Thestapling assembly of claim 1, wherein the adjunct includes a pluralityof openings.
 8. The stapling assembly of claim 1, wherein the first andsecond plurality of struts are formed of a first fused bioabsorbablepolymer, and wherein the nodes are formed of a second fusedbioabsorbable polymer that differs from the first fused bioabsorbablepolymer.
 9. The stapling assembly of claim 1, wherein the at least onefused bioabsorbable polymer is selected from the group consisting ofthermoplastic absorbable polyurethane, ultraviolet curable absorbablepolyurethane, poly(lactic acid), polycaprolactone, polyglycolide,polydioxanone, poly(lactic-co-glycolic acid), polyglycolic acid,trimethylene carbonate, glycolide, dioxanone, polyester, copolymersthereof, and combinations thereof.
 10. A stapling assembly for use witha surgical stapler, comprising: a body having a first end and a secondend, and a longitudinal axis extending therebetween, wherein the bodyhas a slot that extends into and along at least a portion of thelongitudinal axis and configured to receive a cutting element; and athree-dimensional compressible adjunct formed from a matrix comprisingat least one fused bioabsorbable polymer, the adjunct havinginterconnected planar struts that form a lattice structure having firstand second longitudinal portions that are connected by at least onebridging member, wherein the at least one bridging member is configuredto facilitate advancement of the cutting element through the adjunct;and wherein the first and second longitudinal portions each include aplurality of struts interconnected at nodes to form a plurality of trussstructures.
 11. The stapling assembly of claim 10, wherein, when theadjunct is releasably retained on the body, the at least one bridgingmember extends across the slot in a lateral direction relative to thelongitudinal axis of the body such that distal advancement of thecutting element cuts through the at least one bridging member.
 12. Thestapling assembly of claim 10, wherein the at least one fusedbioabsorbable polymer includes a first fused bioabsorbable polymer and asecond fused bioabsorbable polymer that is stiffer than the first fusedbioabsorbable polymer, and wherein the first and second portions areformed of the first fused bioabsorbable polymer and the at least onebridging member is formed of the second fused bioabsorbable polymer. 13.The stapling assembly of claim 10, wherein the body further comprises aplurality of staples disposed therein, and wherein the plurality ofstaples are configured to be deployed into tissue such that the adjunctcan be attached to tissue by the plurality of staples.
 14. The staplingassembly of claim 13, wherein the adjunct has an undeformed state inwhich a maximum height of the adjunct is greater than a maximum heightof the plurality of staples in a formed configuration when the staplesare deployed into tissue.
 15. The stapling assembly of claim 10, whereinthe adjunct is configured to apply a stress of at least about 3 g/mm² tothe tissue stapled thereto for at least 3 days when the adjunct is in atissue deployed state.
 16. The stapling assembly of claim 10, whereinthe adjunct includes a plurality of openings.
 17. The stapling assemblyof claim 10, wherein the at least one fused bioabsorbable polymer isselected from the group consisting of thermoplastic absorbablepolyurethane, ultraviolet curable absorbable polyurethane, poly(lacticacid), polycaprolactone, polyglycolide, polydioxanone,poly(lactic-co-glycolic acid), polyglycolic acid, trimethylenecarbonate, glycolide, dioxanone, polyester, copolymers thereof, andcombinations thereof.